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源于节节麦的合成小麦中抗黑森瘿蚊基因的遗传特征及分子定位

Genetic characterization and molecular mapping of Hessian fly resistance genes derived from Aegilops tauschii in synthetic wheat.

作者信息

Wang Tao, Xu Steven S, Harris Marion O, Hu Jinguo, Liu Liwang, Cai Xiwen

机构信息

Department of Plant Science, North Dakota State University, Fargo, ND 58105, USA.

出版信息

Theor Appl Genet. 2006 Aug;113(4):611-8. doi: 10.1007/s00122-006-0325-z. Epub 2006 Jun 15.

Abstract

Two synthetic hexaploid wheat lines (xAegilotriticum spp., 2n = 6x = 42, genomes AABBDD), SW8 and SW34, developed from the crosses of the durum wheat cultivar Langdon (Triticum turgidum L. var. durum, 2n = 4x = 28, genomes AABB) with two Aegilops tauschii Cosson accessions (2n = 2x = 14, genome DD), were determined to carry Hessian fly [Mayetiola destructor (Say)] resistance genes derived from the Ae. tauschii parents. SW8 was resistant to the Hessian fly biotype Great Plains (GP) and strain vH13 (virulent to H13). SW34 was resistant to biotype GP, but susceptible to strain vH13. Allelism tests indicated that resistance genes in SW8 and SW34 may be allelic to H26 and H13 or correspond to paralogs at both loci, respectively. H26 and H13 were localized to chromosome 4D and 6D, respectively, in previous studies. Molecular mapping in the present study, however, assigned the H26 locus to chromosome 3D rather than 4D. On the other hand, mapping of the resistance gene in SW34 verified the previous assignment of the H13 locus to chromosome 6D. Linkage analysis and physical mapping positioned the H26 locus to the chromosomal deletion bin 3DL3-0.81-1.00. A linkage map for each of these two resistance genes was constructed using simple sequence repeat (SSR) and target region amplification polymorphism (TRAP) markers.

摘要

两个人工合成的六倍体小麦品系(xAegilotriticum spp.,2n = 6x = 42,基因组AABBDD),即SW8和SW34,由硬粒小麦品种兰登(Triticum turgidum L. var. durum,2n = 4x = 28,基因组AABB)与两个节节麦(Aegilops tauschii Cosson)材料(2n = 2x = 14,基因组DD)杂交培育而成,经测定携带源自节节麦亲本的黑森瘿蚊[Mayetiola destructor (Say)]抗性基因。SW8对黑森瘿蚊生物型大平原(GP)和菌株vH13(对H13有毒性)具有抗性。SW34对生物型GP具有抗性,但对菌株vH13敏感。等位性测试表明,SW8和SW34中的抗性基因可能分别与H26和H13等位,或对应于两个位点的旁系同源基因。在先前的研究中,H26和H13分别定位到4D染色体和6D染色体上。然而,本研究中的分子定位将H26位点定位到3D染色体而非4D染色体。另一方面,SW34中抗性基因的定位验证了先前将H13位点定位到6D染色体的结果。连锁分析和物理定位将H26位点定位到染色体缺失区间3DL3 - 0.81 - 1.00。使用简单序列重复(SSR)和目标区域扩增多态性(TRAP)标记构建了这两个抗性基因各自的连锁图谱。

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